Reacción #5392

ord-be1ccb7d1f2e45ccb333bd9c40dea672

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    FiltraciónThe precipitated magnesium salts were filtered
  2. 2
    workup.ADDITIONThe filtrate was diluted with water
  3. 3
    Extracciónextracted with ether
  4. 4
    Lavadowashed with water
  5. 5
    Secadodried over anhydrous sodium sulfate
  6. 6
    FiltraciónThe sodium sulfate was filtered
  7. 7
    Otrothe ether evaporated in vacuo
  8. 8
    Otroto give a brownish solid
  9. 9
    OtroThe brownish solid was recrystallized from isopropanol

Procedimiento

A mixture of 16 g of 3-bromoaniline, 15 g magnesium oxide and 31.8 g benzylbromide in 100 mL dry dimethylformamide was stirred for 47 hours at room temperature, under nitrogen. The precipitated magnesium salts were filtered. The filtrate was diluted with water and extracted with ether. The ether extracts were combined, washed with water and dried over anhydrous sodium sulfate. The sodium sulfate was filtered and the ether evaporated in vacuo to give a brownish solid. The brownish solid was recrystallized from isopropanol to yield 20.75 g of N,N-dibenzyl-3-bromoaniline as a white solid. The structure was confirmed by NMR.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05244771uspto-grants-1993_09